Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07006142

Effect of Prolonged Fasting Time on Gastric Residual Volume in Patients Taking GLP1 Receptor Agonists

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
150 (estimated)
Sponsor
Mayo Clinic · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to determine whether a modified fasting protocol can reduce the potential risk of aspiration for patients currently prescribed GLP1-RAs.

Detailed description

The overall objective of this project is to identify a reasonable means by which patients on GLP1-RAs can be safely cared for in the perioperative period that can be agreed upon by all groups involved in perioperative patient care. This will be assessed in patients undergoing upper endoscopy specifically since assessment of gastric contents would be minimally invasive for this patient population receiving anesthetic care.

Conditions

Interventions

TypeNameDescription
OTHERModified Fasting GuidelinesPatients will follow a full-liquid diet 48 hours prior to their procedure, clear liquid diet 24 hours prior to their procedure, and nothing by mouth (NPO) after midnight on the day of their procedure

Timeline

Start date
2025-08-01
Primary completion
2026-04-30
Completion
2026-04-30
First posted
2025-06-05
Last updated
2026-02-03

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT07006142. Inclusion in this directory is not an endorsement.